US12479720B1ActiveUtility
Method of hydrogen generation through sodium borohydride hydrolysis using CaV2O6@CaSiO3@g-C3N4 nanocomposite
Assignee: IMAM MOHAMMAD IBN SAUD ISLAMIC UNIVPriority: Jul 11, 2025Filed: Jul 11, 2025Granted: Nov 25, 2025
Est. expiryJul 11, 2045(~19 yrs left)· nominal 20-yr term from priority
Inventors:Mohamed Nady Abd El-Hameed IbrahimMohamed Khairy Abdel Fattah OmranBabiker Yagoub Elhadi AbdulkhairFaisal K. Algethami
C01B 3/06C01B 3/065B01J 37/04B01J 23/02B01J 35/647B01J 35/633B01J 21/18B01J 37/346C01B 2203/1082C01B 3/04Y02E60/36
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References
20
Claims
Abstract
A method of generating hydrogen includes contacting a graphite-phase carbon nitride, calcium metavanadate and calcium silicate (CaV2O6@CaSiO3@g-C3N4) nanocomposite with sodium borohydride (NaBH4) in water and hydrolyzing the sodium borohydride to generate hydrogen.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1 . A method for hydrogen generation, comprising:
contacting a graphite-phase carbon nitride calcium metavanadate and calcium silicate (CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 ) nanocomposite with sodium borohydride in water; and hydrolyzing the sodium borohydride to generate hydrogen.
2 . The method of claim 1 , wherein the sodium borohydride is present in an amount of 0.5 to 1 grams (g) per 0.4 milligram (mg) of the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite.
3 . The method of claim 1 , wherein the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite is present in an amount of 3.5 to 4.5 mg per 700 mg of the borohydride.
4 . The method of claim 1 , wherein the contacting occurs at a temperature of 20 to 45 degrees Celsius (° C.).
5 . The method of claim 1 , wherein the hydrogen is generated at a hydrogen generation rate of 2200 to 2400 milliliters per minute (mL/min) per gram of CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite at a temperature of 35° to 40° C.
6 . The method of claim 1 , wherein the hydrolyzing generates at least 10 mL hydrogen within 2 minutes at a temperature of 35° to 40° C.
7 . The method of claim 1 , wherein the hydrolyzing generates at least 30 mL hydrogen within 3 minutes at a temperature of 35° to 40° C.
8 . The method of claim 1 , wherein the hydrolyzing generates at least 45 mL hydrogen within 5 minutes at a temperature of 35° to 40° C.
9 . The method of claim 1 , wherein the hydrogen is generated at a hydrogen generation rate of 300 to 400 mL/min per gram of CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite at a temperature of 25° to 30° C.
10 . The method of claim 1 , wherein the hydrolyzing generates at least 5 mL hydrogen within 2 minutes at a temperature of 25° to 30° C.
11 . The method of claim 1 , wherein the hydrolyzing generates at least 21 mL hydrogen within 5 minutes at a temperature of 25° to 30° C.
12 . The method of claim 1 , wherein the hydrolyzing generates at least 43 mL hydrogen within 10 minutes at a temperature of 25° to 30° C.
13 . The method of claim 1 , wherein the hydrolyzing at a temperature of 35° to 40° C. has a hydrogen generation rate that is 8 to 11 times faster than the hydrolyzing without contacting with the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite.
14 . The method of claim 1 , wherein the hydrolyzing at a temperature of 25° to 30° C. has a hydrogen generation rate that is 4 to 6 times faster than the hydrolyzing without contacting with the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite.
15 . The method of claim 1 , wherein the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite comprises a graphite-phase carbon nitride (g-C 3 N 4 ) in an amount of 20 to 40 percent by weight (wt. %), calcium silicate (CaSiO 3 ) in an amount of 20 to 40 wt. %, and calcium metavanadate (CaV 2 O 6 ) in an amount of 20 to 40 wt. %, based on a total weight of the CaV 2 O 6 /CaSiO 3 /g-C 3 N 4 nanocomposite.
16 . The method of claim 1 , wherein the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite is porous, and has an average pore diameter of 2 to 16 nanometers (nm).
17 . The method of claim 1 , wherein the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite is porous, and has a pore volume to 0.2 to 0.24 cubic centimeters per gram (cm 3 g −1 ).
18 . The method of claim 1 , wherein the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite comprises:
a major CaV 2 O 6 phase; a major CaSiO 3 phase; and a minor g-C 3 N 4 phase, wherein the CaV 2 O 6 phase and the CaSiO 3 phase are in a structure of nanowires, and the g-C 3 N 4 phase is in a structure of nanosheets, wherein the nanowires are dispersed in between the nanosheets.
19 . The method of claim 1 , wherein the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite has g-C 3 N 4 nanosheets with an interplanar spacing of 0.13 to 0.25 nanometers (nm).
20 . The method of claim 1 , wherein the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite is produced in a process, comprising:
mixing a calcium salt and a metasilicate salt in a solvent to form a silicate product; heating urea to form g-C 3 N 4 product; heating ammonium metavanadate with xylose in nitric acid to form vanadate product; microwaving the silicate product, the g-C 3 N 4 product, and the vanadate product in an organic solvent to form the CaV 2 O 6 @CaSiO 3 @g-C 3 N 4 nanocomposite.Join the waitlist — get patent alerts
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